EP3468604B1 - Pharmaceutical combinations for treating cancer - Google Patents

Pharmaceutical combinations for treating cancer Download PDF

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EP3468604B1
EP3468604B1 EP17726974.3A EP17726974A EP3468604B1 EP 3468604 B1 EP3468604 B1 EP 3468604B1 EP 17726974 A EP17726974 A EP 17726974A EP 3468604 B1 EP3468604 B1 EP 3468604B1
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cancer
alkyl
cycloalkyl
pharmaceutical combination
hydrogen
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EP3468604A1 (en
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Alexander Bausch
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Support-Venture GmbH
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

  • the present invention relates to pharmaceutical combinations comprising a PPAR agonist and a P38 inhibitor for use in a method for the prevention, delay of progression or treatment of cancer in a subject.
  • cancer is still the third most common cause of death worldwide after cardiovascular diseases and infectious/parasitic diseases; in absolute numbers, this corresponds to 7.6 million deaths (ca. 13% of all deaths) in any given year.
  • the WHO estimates deaths due to cancer to increase to 13.1 million by 2030, while the American Cancer Society expects over 1,685,210 new cancer cases diagnosed and 595,690 cancer deaths in the US in 2016.
  • a 2012 survey by McMillan Cancer Support in the UK has revealed that the median survival time of cancer patients overall has increased from 1 year to 6 years since the 1970's.
  • median survival has barely improved, remaining less than one year.
  • a combination comprising a PPAR agonist, such as pioglitazone and a P38 inhibitor, such as pamapimod is useful for the prevention, delay of progression or treatment of cancer, in particular lung cancer, ovarian cancer, prostate cancer, breast cancer, bladder cancer, liver cancer, cancer of the gastrointestinal tract, hematological cancer or kidney cancer.
  • a P38 inhibitor such as pamapimod
  • the present invention provides a pharmaceutical combination comprising:
  • the present invention provides such a pharmaceutical combination as described herein, for use as a medicament.
  • the present invention provides such a pharmaceutical combination as described herein, for use in a method for the prevention, delay of progression or treatment of cancer in a subject.
  • the present invention provides a pharmaceutical combination comprising:
  • the present invention provides pharmaceutical combinations comprising a PPAR agonist, such as pioglitazone and the P38 inhibitor, such as pamapimod, which are useful for the prevention, delay of progression, or treatment of cancer.
  • a PPAR agonist such as pioglitazone
  • the P38 inhibitor such as pamapimod
  • the present invention provides a pharmaceutical combination comprising:
  • the terms “individual,” “subject” or “patient” are used herein interchangeably.
  • the subject is a mammal.
  • Mammals include, but are not limited to primates (including human and non-human primates).
  • the subject is a human.
  • the terms "cancer” and “cancerous” as used herein refer to or describe the physiological condition in mammals that is typically characterized by unregulated cell growth.
  • a “tumor” comprises one or more cancerous cells. Examples of cancer include, but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia or lymphoid malignancies.
  • cancers include squamous cell cancer (e.g., epithelial squamous cell cancer), lung cancer including small- cell lung cancer, non-small cell lung cancer ("NSCLC”), adenocarcinoma of the lung and squamous carcinoma of the lung, cancer of the peritoneum, hepatocellular cancer, gastric or stomach cancer including gastrointestinal cancer, pancreatic cancer, glioblastoma, cervical cancer, ovarian cancer, liver cancer, bladder cancer, hepatoma, breast cancer, cancer of the gastrointestinal (GI) tract, endometrial or uterine carcinoma, salivary gland carcinoma, kidney or renal cancer, prostate cancer, vulval cancer, thyroid cancer, hepatic carcinoma, anal carcinoma, penile carcinoma, as well as head and neck cancer.
  • GI gastrointestinal
  • metastatic cancer means the state of cancer, e.g. the state of lung cancer or cancer of the gastrointestinal (GI) tract where the cancer cells are transmitted from the original site to one or more sites elsewhere in the body, by the blood vessels or lymphatics, to form one or more secondary tumors at one or more sites or organs besides the original site or organ.
  • GI gastrointestinal
  • PPAR agonist refers to a drug that is activating peroxisome proliferator activated receptor (PPAR) such as PPAR gamma receptor, PPAR alpha receptor, PPAR delta receptor or combinations thereof.
  • PPAR peroxisome proliferator activated receptor
  • the PPAR agonist according to the invention is activating PPAR gamma.
  • said PPAR agonist is a PPAR gamma agonist selected from a list comprising pioglitazone, troglitazone and rosiglitazone or a pharmaceutically acceptable salt thereof; or a PPAR alpha agonist selected from a list comprising fibrates such as fenofibrate (fenofibric acid), clofibrate or gemfibrozil or a pharmaceutically acceptable salt thereof; or a PPAR dual agonist (PPAR alpha/gamma or PPAR alpha/delta agonists) selected from a list comprising aleglitazar, muraglitazar, tesaglitazar, ragaglitazar, saroglitazar, GFT505 and naveglitazar or a pharmaceutically acceptable salt thereof; or a PPAR delta agonist such as GW501516 or a pharmaceutically acceptable salt thereof; or a PPAR pan agonists (PPAR alpha/delta/gamma agonist selected
  • PPAR gamma agonists PPAR modulators, PPAR alpha agonists and/or PPAR alpha/gamma dual agonists are used in the context of the present invention.
  • PPAR gamma agonists PPAR alpha agonists and/or PPAR alpha/gamma dual agonists
  • more particular PPAR gamma agonists are used in the context of the present invention.
  • the PPAR agonist according to the invention is a PPAR gamma agonist or modulator selected from the group consisting of pioglitazone, rosiglitazone, troglitazone, INT131 or a pharmaceutically acceptable salt thereof.
  • said PPAR agonist is a PPAR gamma agonist selected from the group consisting of pioglitazone, rosiglitazone and troglitazone or a pharmaceutically acceptable salt thereof.
  • said PPAR agonist is pioglitazone or a pharmaceutically acceptable salt thereof, e.g. pioglitazone hydrochloride.
  • said PPAR agonist is a PPAR alpha agonist selected from the group consisting of fenofibrate (fenofibric acid), clofibrate and gemfibrozil, preferably fenofibrate (fenofibric acid) or a pharmaceutically acceptable salt thereof.
  • said PPAR agonist is a PPAR alpha/gamma dual agonist selected from the group consisting of aleglitazar, muraglitazar, tesaglitazar, ragaglitazar, saroglitazar, GFT505 and naveglitazar or a pharmaceutically acceptable salt thereof, preferably muraglitazar or tesaglitazar or a pharmaceutically acceptable salt thereof.
  • Pioglitazone is described e.g. in US Patent No. 4,687,777 or in Dormandy JA, Charbonnel B, Eckland DJ, Erdmann E, Massi-Benedetti M, Moules IK, Skene AM, Tan MH, Lefèbvre PJ, Murray GD, Standl E, Wilcox RG, Wilhelmsen L, Betteridge J, Birkeland K, Golay A, Heine RJ, Korányi L, Laakso M, Mokán M, Norkus A, Pirags V, Podar T, Scheen A, Scherbaum W, Schernthaner G, Schmitz O, Skrha J, Smith U, Taton J; PROactive investigators. Lancet. 2005 Oct 8;366(9493): 1279-89 , and is represented by the structural formula indicated below:
  • Troglitazone is described e.g. in Florez JC, Jablonski KA, Sun MW, Bayley N, Kahn SE, Shamoon H, Hamman RF, Knowler WC, Nathan DM, Altshuler D; Diabetes Prevention Program Research Group. J Clin Endocrinol Metab. 2007 Apr;92(4): 1502-9 and is represented by the structural formula indicated below:
  • Rosiglitazone is described e.g. in Nissen SE, Wolski K. N Engl J Med. 2007 Jun 14;356(24):2457-71 . Erratum in: N Engl J Med. 2007 Jul 5;357(1): 100 .
  • Fenofibrate is described e.g. in Bonds DE, Craven TE, Buse J, Crouse JR, Cuddihy R, Elam M, Ginsberg HN, Kirchner K, Marcovina S, Mychaleckyj JC, O'Connor PJ, Sperl-Hillen JA. Diabetologia. 2012 Jun;55(6):1641-50 and is represented by the structural formula indicated below:
  • Clofibrate is described e.g. in Rabkin SW, Hayden M, Frohlich J. Atherosclerosis. 1988 Oct;73(2-3):233-40 and is represented by the structural formula indicated below:
  • Fenofibrate (fenofibric acid) is described e.g. in Schima SM, Maciejewski SR, Hilleman DE, Williams MA, Mohiuddin SM. Expert Opin Pharmacother. 2010 Apr; 11(5):731-8 and is represented by the structural formula indicated below:
  • Gemfibrozil is described e.g. in Adabag AS, Mithani S, Al Aloul B, Collins D, Bertog S, Bloomfield HE; Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group. Am Heart J. 2009 May; 157(5):913-8 and is represented by the structural formula indicated below:
  • Aleglitazar is described e.g. in Lincoff AM, Tardif JC, Schwartz GG, Nicholls SJ, Rydén L, Neal B, Malmberg K, Wedel H, Buse JB, Henry RR, Weichert A, Cannata R, Svensson A, Volz D, Grobbee DE; AleCardio Investigators. JAMA. 2014 Apr 16;311(15):1515-25 and is represented by the structural formula indicated below:
  • Muraglitazar is described e.g. in Fernandez M, Gastaldelli A, Triplitt C, Hardies J, Casolaro A, Petz R, Tantiwong P, Musi N, Cersosimo E, Ferrannini E, DeFronzo RA. Diabetes Obes Metab. 2011 Oct;13(10):893-902 and is represented by the structural formula indicated below:
  • Tesaglitazar is described e.g. in Bays H, McElhattan J, Bryzinski BS; GALLANT 6 Study Group. Diab Vasc Dis Res. 2007 Sep;4(3):181-93 and is represented by the structural formula indicated below:
  • Ragaglitazar is described e.g. in Saad MF, Greco S, Osei K, Lewin AJ, Edwards C, Nunez M, Reinhardt RR; Ragaglitazar Dose-Ranging Study Group. Diabetes Care. 2004 Jun;27(6):1324-9 and is represented by the structural formula indicated below:
  • Saroglitazar is described e.g. in Agrawal R. Curr Drug Targets. 2014 Feb;15(2):151-5 . and is represented by the structural formula indicated below:
  • Naveglitazar is described e.g. in Ahlawat P, Srinivas NR. Eur J Drug Metab Pharmacokinet. 2008 Jul-Sep;33(3):187-90 .
  • GW501516 is described e.g. in Wang X, Sng MK, Foo S, Chong HC, Lee WL, Tang MB, Ng KW, Luo B, Choong C, Wong MT, Tong BM, Chiba S, Loo SC, Zhu P, Tan NS. J Control Release. 2015 Jan 10;197:138-47 and is represented by the structural formula indicated below:
  • GFT505 is described e.g. in Cariou B, Staels B. Expert Opin Investig Drugs. 2014 Oct;23(10): 1441-8 and is represented by the structural formula indicated below:
  • INT131 is described e.g. in. Taygerly JP, McGee LR, Rubenstein SM, Houze JB, Cushing TD, Li Y, Motani A, Chen JL, Frankmoelle W, Ye G, Learned MR, Jaen J, Miao S, Timmermans PB, Thoolen M, Kearney P, Flygare J, Beckmann H, Weiszmann J, Lindstrom M, Walker N, Liu J, Biermann D, Wang Z, Hagiwara A, Iida T, Aramaki H, Kitao Y, Shinkai H, Furukawa N, Nishiu J, Nakamura M. Bioorg Med Chem. 2013 Feb 15;21(4):979-92 and is represented by the structural formula indicated below:
  • PPAR activation by the PPAR agonist is usually strong in the low nanomolar range to low micromolar range, e.g in a range of 0.1 nM to 100 ⁇ M.
  • the PPAR activation is weak or partial, i.e. a PPAR agonist is used in the methods of the present invention which yields maximal activation of PPAR-receptor in a reporter assay system of 10% to 100% compared to a reference PPAR agonist which is known to causes a maximum PPAR activation.
  • p38 inhibitor refers to a drug that is inhibiting a p38 mitogen-activated protein (MAP) kinase, such as p38- ⁇ (MAPK14), p38- ⁇ (MAPK11), p38- ⁇ (MAPK12 / ERK6), and/or p38- ⁇ (MAPK13 / SAPK4).
  • MAP mitogen-activated protein
  • the p38 inhibitors of the claimed invention are compounds of formulae I and II or pharmaccutically acceptable salts thereof, wherein
  • the p38 inhibitor according to the invention is a compound of formula I or pharmaceutically acceptable salts thereof, wherein
  • the p38 inhibitor according to the invention is a compound of formula I wherein X 1 is NR 4 and X 2 is NR 7 or X 1 and X 2 are each O, wherein R 4 and R 7 are as defined above.
  • the p38 inhibitor according to the invention is a compound of formula I wherein W is NR 2 , wherein R 2 is hydrogen, alkyl, acyl or alkoxycarbonyl, preferably hydrogen or alkyl, more preferably hydrogen.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 1 is hydrogen, alkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, heteroalkylsubstituted cycloalkyl, heterosubstituted cycloalkyl, heteroalkyl, cyanoalkyl, heterocyclyl, heterocyclylalkyl or (heterocyclyl)(cycloalkyl)alkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 1 is hydrogen, alkyl, haloalkyl, heteroalkyl or cyanoalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 1 is cycloalkyl, cycloalkylalkyl, heteroalkylsubstituted cycloalkyl, heterosubstituted cycloalkyl, heterocyclyl, heterocyclylalkyl or (heterocyclyl)(cycloalkyl)alkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroalkyl, cyanoalkyl, alkylene-C(O)-R 31 (where R 31 is hydrogen, alkyl, hydroxy, alkoxy, amino, monoalkylamino or dialkylamino) or acyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is hydrogen, alkyl, haloalkyl, heteroalkyl, cyanoalkyl, cycloalkyl or cycloalkylalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is hydrogen, alkyl, haloalkyl, heteroalkyl or cyanoalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is cycloalkyl or cycloalkylalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein X 1 and X 2 are both O.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 1 is alkyl or heteroalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 1 is heteroalkyl, preferably 3-hydroxy-1-(2-hydroxyethyl)-propyl or 2-hydroxy-1-methylethyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is alkyl or heteroalkyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is alkyl, preferably methyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein R 3 is heteroalkyl, preferably 2-hydroxy-propyl.
  • the p38 inhibitor according to the invention is a compound of formula I wherein W is NH.
  • the p38 inhibitor according to the invention is a compound of formula I wherein Z is N.
  • the p38 inhibitor according to the invention is a compound of formula I wherein Ar 1 is aryl, preferably substituted aryl, more preferably aryl substituted with two halo substituents, most preferably aryl substituted with two halo substituents in ortho and para position.
  • the p38 inhibitor according to the invention is a compound of formula I wherein X 1 is NR 4 and X 2 is NR 7 or X 1 and X 2 are each O, wherein R 4 and R 7 are as defined above; and wherein
  • the p38 inhibitor according to the invention is a compound of formula I wherein X 1 and X 2 are each O and wherein Z is N and wherein W is NH and wherein Ar 1 is substituted aryl and wherein R 1 is heteroalkyl and wherein R 3 is alkyl or heteroalkyl.
  • the p38 inhibitor according to the invention is pamapimod, having the chemical name 6-(2,4-Difluorophenoxy)-2-[3-hydroxy-1-(2-hydroxyethyl)-propylamino]-8-methyl-8 H -pyrido[2,3- d ]pyrimidin-7-one and the chemical formula III or a pharmaceutically acceptable salt thereof.
  • the p38 inhibitor according to the invention is R9111, having the chemical name 6-(2,4-Difluorophenoxy)-2-[( S )-2-hydroxy-1-methyl-ethylamino]-8-[( S )-2-hydroxy-propyl]-8 H -pyrido[2,3- d ]pyrimidin-7-one and the chemical formula IV or a pharmaceutically acceptable salt thereof.
  • p38 inhibitors mentioned herein are pamapimod, losmapimod, dilmapimod, AZD7624, ARRY-371797, LY2228820, R9111, PH-797804, BIRB 796, VX-702, VX-745 SB 239063, SB202190, SCIO 469, and BMS 582949 or a pharmaceutically acceptable salt thereof.
  • Pamapimod and its synthesis are described e.g. in WO2008/151992 and in WO2002/064594 and in e.g. Hill RJ, Dabbagh K, Phippard D, Li C, Suttmann RT, Welch M, Papp E, Song KW, Chang KC, Leaffer D, Kim Y-N, Roberts RT, Zabka TS, Aud D, Dal Porto J, Manning AM, Peng SL, Goldstein DM, and Wong BR; Pamapimod, a Novel p38 Mitogen-Activated Protein Kinase Inhibitor: Preclinical Analysis of Efficacy and Selectivity J Pharmacol Exp Ther. December 2008 327:610-619 .
  • Losmapimod is described in e.g. Cheriyan J, Webb AJ, Sarov-Blat L, Elkhawad M, Wallace SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland SM, Switzerland, Collier DJ, Morgan J, Fang Z, Willette RN, Lepore JJ, Cockcroft JR, Sprecher DL, Wilkinson IB. Inhibition of p38 mitogen-activated protein kinase improves nitric oxide-mediated vasodilatation and reduces inflammation in hypercholesterolemia. Circulation. 2011 Feb 8;123(5):515-23 , and is represented by the structural formula indicated below:
  • Dilmapimod is described in e.g. Christie JD, Vaslef S, Chang PK, May AK, Gunn SR, Yang S, Hardes K, Kahl L, Powley WM, Lipson DA, Bayliffe AI, Lazaar AL.
  • LY2228820 is described in e.g. Campbell RM, Anderson BD, Brooks NA, Brooks HB, Chan EM, De Dios A, Gilmour R, Graff JR, Jambrina E, Mader M, McCann D, Na S, Parsons SH, Pratt SE, Shih C, Stancato LF, Starling JJ, Tate C, Velasco JA, Wang Y, Ye XS. Characterization of LY2228820 dimesylate, a potent and selective inhibitor of p38 MAPK with antitumor activity. Mol Cancer Ther. 2014 Feb;13(2):364-74 , and is represented by the structural formula indicated below:
  • AZD7624 is described in Patel N, Cunoosamy D, Hegelund-Myrback T, Pehrson R, Taib Z, Jansson P, Lundin S, Greenaway S, Clarke G, Siew L. AZD7624, an inhaled p38 inhibitor for COPD, attenuates lung and systemic inflammation after LPS Challenge in humans. Eur Resp J. DOI: 10.1183/13993003.1 Sept 2015 .
  • ARRY-371797 is described in e.g. Muchir A, Wu W, Choi JC, Iwata S, Morrow J, Homma S, Worman HJ. Abnormal p38 ⁇ mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation.
  • Hum Mol Genet. 2012 Oct 1;21(19):4325-33 and is represented by the structural formula indicated below:
  • PH-797804 is described in e.g. Xing L, Devadas B, Devraj RV, Selness SR, Shieh H, Walker JK, Mao M, Messing D, Samas B, Yang JZ, Anderson GD, Webb EG, Monahan JB. Discovery and characterization of atropisomer PH-797804, a p38 MAP kinase inhibitor, as a clinical drug candidate. ChemMedChem. 2012 Feb 6;7(2):273-80 , and is represented by the structural formula indicated below:
  • BIRB 796 is described in e.g. Dietrich J, Hulme C, Hurley LH. The design, synthesis, and evaluation of 8 hybrid DFG-out allosteric kinase inhibitors: a structural analysis of the binding interactions of Gleevec, Nexavar, and BIRB-796. Bioorg Med Chem. 2010 Aug 1;18(15):5738-48 , and is represented by the structural formula indicated below:
  • VX-702 is described in e.g. Damjanov N, Kauffman RS, Spencer-Green GT. Efficacy, pharmacodynamics, and safety of VX-702, a novel p38 MAPK inhibitor, in rheumatoid arthritis: results of two randomized, double-blind, placebo-controlled clinical studies. Arthritis Rheum. 2009 May;60(5):1232-41 , and is represented by the structural formula indicated below:
  • VX-745 is described in e.g. Duffy JP, Harrington EM, Salituro FG, Cochran JE, Green J, Gao H, Bemis GW, Evindar G, Galullo VP, Ford PJ, Germann UA, Wilson KP, Bellon SF, Chen G, Taslimi P, Jones P, Huang C, Pazhanisamy S, Wang YM, Murcko MA, Su MS.
  • the Discovery of VX-745 A Novel and Selective p38 ⁇ Kinase Inhibitor. ACS Med Chem Lett. 2011 Jul 28;2(10):758-63 , and is represented by the structural formula indicated below:
  • SB239063 is described in e.g. Strassburger M, Braun H, Reymann KG. Anti-inflammatory treatment with the p38 mitogen-activated protein kinase inhibitor SB239063 is neuroprotective, decreases the number of activated microglia and facilitates neurogenesis in oxygen-glucose-deprived hippocampal slice cultures. Eur J Pharmacol. 2008 Sep 11;592(1-3):55-61 , and is represented by the structural formula indicated below:
  • SB202190 is described in e.g. Hirosawa M, Nakahara M, Otosaka R, Imoto A, Okazaki T, Takahashi S.
  • the p38 pathway inhibitor SB202190 activates MEK/MAPK to stimulate the growth of leukemia cells. Leuk Res. 2009 May;33(5):693-9 , and is represented by the structural formula indicated below:
  • SCIO469 is described in e.g. Sokol L, Cripe L, Kantarjian H, Sekeres MA, Parmar S, Greenberg P, Goldberg SL, Bhushan V, Shammo J, Hohl R, Verma A, Garcia-Manero G, Li YP, Lowe A, Zhu J, List AF. Randomized, dose-escalation study of the p38 ⁇ MAPK inhibitor SCIO-469 in patients with myelodysplastic syndrome. Leukemia. 2013 Apr;27(4):977-80 , and is represented by the structural formula indicated below:
  • BMS 582949 is described in e.g. Liu C, Lin J, Wrobleski ST, Lin S, Hynes J, Wu H, Dyckman AJ, Li T, Wityak J, Gillooly KM, Pitt S, Shen DR, Zhang RF, McIntyre KW, Salter-Cid L, Shuster DJ, Zhang H, Marathe PH, Doweyko AM, Sack JS, Kiefer SE, Kish KF, Newitt JA, McKinnon M, Dodd JH, Barrish JC, Schieven GL, Leftheris K.
  • composition comprising
  • composition comprising
  • composition comprising
  • composition comprising
  • composition comprising
  • composition comprising
  • composition comprising
  • the invention relates to a pharmaceutical combination
  • a pharmaceutical combination comprising a PPAR agonist, such as pioglitazone or a pharmaceutically acceptable salt thereof and the p38 inhibitor, such as pamapimod or a pharmaceutically acceptable salt thereof.
  • a pharmaceutical combination according to the invention is for example a combined preparation or a pharmaceutical composition, for simultaneous, separate or sequential use.
  • combined preparation defines especially a "kit of parts” in the sense that said PPAR agonist and said p38 inhibitor can be dosed independently, either in separate form or by use of different fixed combinations with distinguished amounts of the active ingredients.
  • the ratio of the amount of PPAR agonist to the amount of p38 inhibitor to be administered in the combined preparation can be varied, e.g. in order to cope with the needs of a patient sub-population to be treated or the needs of a single patient, which needs can be different due to age, sex, body weight, etc. of a patient.
  • the individual parts of the combined preparation (kit of parts) can be administered simultaneously or sequentially, i.e. chronologically staggered, e.g. at different time points and with equal or different time intervals for any part of the kit of parts.
  • composition refers to a fixed-dose combination (FDC) that includes the PPAR agonist and the p38 inhibitor combined in a single dosage form, having a predetermined combination of respective dosages.
  • FDC fixed-dose combination
  • additive-on therapy means an assemblage of reagents for use in therapy, the subject receiving the therapy begins a first treatment regimen of one or more reagents prior to beginning a second treatment regimen of one or more different reagents in addition to the first treatment regimen, so that not all of the reagents used in the therapy are started at the same time. For example, adding the p38 inhibitor therapy to a patient already receiving PPAR agonist therapy.
  • the pharmaceutical combination according to the invention is a pharmaceutical composition, i.e. a fixed-dose combination.
  • the pharmaceutical combination according to the invention is a combined preparation.
  • the amount of the PPAR agonist and the p38 inhibitor to be administered will vary depending upon factors such as the particular compound, disease condition and its severity, according to the particular circumstances surrounding the case, including, e.g., the specific PPAR agonist being administered, the route of administration, the condition being treated, the target area being treated, and the subject or host being treated.
  • the invention provides a pharmaceutical combination comprising a PPAR agonist and a compound of the formula I or II, wherein said PPAR agonist and said compound of the formula I or II are present in a therapeutically effective amount.
  • an amount capable of invoking one or more of the following effects in a subject receiving the combination of the present invention refers to an amount capable of invoking one or more of the following effects in a subject receiving the combination of the present invention: (i) inhibition or arrest of tumor growth, including, reducing the rate of tumor growth or causing complete growth arrest; (ii) reduction in the number of tumor cells; (iii) reduction in tumor size; (iv) reduction in tumor number; (v) inhibition of metastasis (i.e., reduction, slowing down or complete stopping) of tumor cell infiltration into peripheral organs; (vi) enhancement of antitumor immune response, which may, but does not have to, result in the regression or elimination of the tumor; (vii) relief, to some extent, of one or more symptoms associated with cancer; (viii) increase in progression-free survival (PFS) and/or; overall survival (OS) of the subject receiving the combination.
  • PFS progression-free survival
  • OS overall survival
  • the invention provides a pharmaceutical combination comprising a PPAR agonist and a compound of the formula I or II, wherein said PPAR agonist and said compound of the formula I or II are present in an amount producing an additive therapeutic effect.
  • additive means that the effect achieved with the pharmaceutical combinations of this invention is approximately the sum of the effects that result from using the anti-cancer agents, namely the PPAR agonist and the p38 inhibitor, as a monotherapy.
  • an additive effect provides for greater efficacy at the same doses, and may lead to longer duration of response to the therapy.
  • the invention provides a pharmaceutical combination comprising a PPAR agonist and a compound of the formula I or II, wherein said PPAR agonist and said compound of the formula I or II are present in an amount producing a synergistic therapeutic effect.
  • the term “synergistic” means that the effect achieved with the pharmaceutical combinations of this invention is greater than the sum of the effects that result from using the anti-cancer agents, namely the PPAR agonist and the p38 inhibitor, as a monotherapy.
  • synergy provides for greater efficacy at the same doses, and may lead to longer duration of response to the therapy.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said PPAR agonist in the combination is from about 0.1 to about 50 mg or from about 0.1 to about 45 mg or from about 0.1 to about 30 mg or from about 0.1 to about 15 mg or from about 0.8 to about 10 mg or from about 0.1 to about 5 mg.
  • the invention provides a pharmaceutical combination comprising the J p38 inhibitor and a PPAR agonist, wherein the amount of said PPAR agonist in the combination is about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg or about 10 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and pioglitazone, wherein the amount of pioglitazone in the combination is about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg or about 10 mg.
  • the PPAR agonist is administered to the subject at a dose that is below the dose needed for the treatment of diabetes using a PPAR agonist.
  • the PPAR agonist is administered to the subject at a dose that is a factor of 8-20 fold lower than the top dose approved for the treatment of diabetes, in particular a factor of 8-20 fold lower than the top dose evaluated and tested for the treatment of diabetes in human.
  • the top dose evaluated and tested for the treatment of diabetes in human e.g. for a PPAR gamma agonist such as pioglitazone is usually in the range from about 30-45 mg/day.
  • at the PPAR dose used common side effects seen at doses used in the treatment of diabetes are reduced or not detected.
  • the PPAR agonist is administered to the subject at a dose that is below the active dose for antidiabetic or anti-dyslipidemic effect of said PPAR agonist, in particular a dose that is below the active dose for antidiabetic or anti-dyslipidemic effect of the PPAR agonist in human.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and pioglitazone, wherein the amount of pioglitazone in the combination is below the dose typically needed for the treatment of diabetes with pioglitazone.
  • a typical dosing regimen of pioglitazone in the treatment of diabetes is 15 to 45 mg pioglitazone once-daily.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and pioglitazone, wherein the amount of pioglitazone in the combination is about 5 mg.
  • the invention provides a pharmaceutical combination comprising ; the p38 inhibitor and pioglitazone, wherein the amount of pioglitazone in the combination is about 2 mg.
  • the invention provides a pharmaceutical combination comprising a p38 inhibitor and a PPAR agonist, wherein the amount of said p38 inhibitor in the combination is from about 1 to about 500 mg or from about 1 to about 450 mg or from about 1 to about 400 mg or from about 1 to about 350 mg or from about 1 to about 300 mg or from about 1 to about 250 mg or from about 1 to about 200 mg or from about 1 to about 150 mg or from about 1 to about 125 mg or from about 10 to about 125 mg or from about 10 to about 100 mg or from about 20 to about 100 mg or from about 30 to about 100 mg or from about 40 to about 100 mg or from about 50 to about 100 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said p38 inhibitor in the combination is about 25 mg, about 50 mg, about 75 mg, about 125 mg, about 150 mg or about 300 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said p38 inhibitor in the combination is about 50 mg, about 75 mg, about 100 mg, or about 150 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said p38 inhibitor in the combination is about 75 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said PPAR agonist in the combination is from about 0.1 to about 50 mg or from about 0.1 to about 45 mg or from about 0.1 to about 30 mg or from about 0.1 to about 15 mg or from about 0.8 to about 10 mg; and wherein the amount of said p38 inhibitor in the combination is from about 1 to about 500 mg or from about 1 to about 450 mg or from about 1 to about 400 mg or from about 1 to about 350 mg or from about 1 to about 300 mg or from about 1 to about 250 mg or from about 1 to about 200 mg or from about 1 to about 150 mg or from about 1 to about 125 mg or from about 10 to about 125 mgor from about 10 to about 100 mg or from about 20 to about 100 mg or from about 30 to about 100 mg or from about 40 to about 100 mg or from about 50 to about 100 mg.
  • the invention provides a pharmaceutical combination comprising the p38 inhibitor and a PPAR agonist, wherein the amount of said PPAR agonist in the combination is about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg or about 10 mg; and wherein the amount of said p38 inhibitor in the combination is about 50 mg, about 75 mg, about 100 mg, or about 150 mg.
  • the invention provides a pharmaceutical combination comprising pamapimod and pioglitazone, wherein the amount of pamapimod in the combination is about 75 mg and wherein the amount of pioglitazone in the combination is from about 2 mg to about 5 mg.
  • the invention also relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a PPAR agonist such as pioglitazone and the p38 inhibitor such as pamapimod and at least one pharmaceutically acceptable carrier.
  • pharmaceutically acceptable carrier refers to a carrier or excipient or diluent that is suitable for use with humans and/or animals without undue adverse side effects (such as toxicity, irritation, and allergic response) commensurate with a reasonable benefit/risk ratio. It can be a pharmaceutically acceptable solvent, suspending agent or vehicle, for delivering the instant compounds to the subject.
  • a pharmaceutical combination according to the invention is, preferably, suitable for enteral administration, such as oral or rectal administration to a subject and comprises a therapeutically effective amount of the active ingredients and one or more suitable pharmaceutically acceptable carrier.
  • a pharmaceutical combination according to the invention is prepared in a manner known per se, e.g. by means of conventional mixing, granulating, coating, dissolving or lyophilizing processes.
  • any of the usual pharmaceutical media may be employed, for example water, glycols, oils, alcohols, carriers, such as starches, sugars, or microcrystalline cellulose, diluents, granulating agents, lubricants, binders, disintegrating agents and the like. Because of their ease of administration, tablets and capsules represent the most advantageous oral dosage unit forms, in which case solid pharmaceutical carriers are obviously employed.
  • the pharmaceutical combination according to the invention is a combination for enteral administration.
  • said pharmaceutical combination is preferably a pharmaceutical composition, i.e. fixed-dose combination.
  • a pharmaceutical combination for enteral administration is, for example, a unit dosage form, such as a tablet, a capsule or a suppository.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a PPAR agonist, such as pioglitazone and the p38 inhibitor, such as pamapimod and at least one pharmaceutically acceptable carrier, wherein the composition is a tablet or a capsule, preferably a tablet.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a PPAR agonist, such as pioglitazone and the p38 inhibitor, such as pamapimod and at least one pharmaceutically acceptable carrier, wherein the composition is a sustained release tablet.
  • the pharmaceutical composition according to the invention is for oral administration, wherein the composition is adapted to provide sustained release of the active pharmaceutical ingredients (API).
  • the composition may increase T max or reduce C max , or both increase T max and reduce C max , as compared to an immediate release composition.
  • C max means the peak concentration of the drug in the plasma.
  • T max means the time from administration to reach C max .
  • a sustained release composition as compared to an immediate release composition comprises one or more agents which act to prolong release of the API; for example, the API may be embedded in a matrix and/or surrounded by a membrane which, in either case, controls (reduces) the rate of diffusion of the API into the Gl tract.
  • hydrophobic polymers for example ethyl cellulose or a methacrylic acid polymer, or a combination thereof.
  • Such polymers may be comprised in a coating or may be included in admixture with the API (i.e. may be used as a matrix-former), or may be present both in a coating and in admixture with the API.
  • insoluble erodible materials for example a wax or a hydrogenated vegetable oil, or a combination thereof.
  • Such materials may be comprised in a coating or may be included in admixture with the API (i.e. may be used as a matrix-former), or may be present both in a coating and in admixture with the API.
  • composition according to the invention may contain, e.g., from about 10% to about 100% of the therapeutically effective amount of the active ingredients.
  • said PPAR agonist need not be administered in the same dosage form as said p38 inhibitor.
  • An exemplary treatment regime entails administration once daily, twice daily, three times daily, every second day, twice per week, once per week.
  • the combination of the invention is usually administered on multiple occasions. Intervals between single dosages can be, for example, less than a day, daily, every second day, twice per week, or weekly.
  • the combination of the invention may be given as a continous uninterrupted treatment.
  • the combination of the invention may also be given in a regime in which the subject receives cycles of treatment interrupted by a drug holiday or period of non-treatment.
  • the combination of the invention may be administered according to the selected intervals above for a continuous period of one week or a part thereof, for two weeks, for three weeks for four weeks, for five weeks or for six weeks and then stopped for a period of one week, or a part thereof, for two weeks, for three weeks, for four weeks, for five weeks, or for six weeks.
  • the combination of the treatment interval and the non-treatment interval is called a cycle.
  • the cycle may be repeated one or more times. Two or more different cycles may be used in combination for repeating the treatment one or more times. Intervals can also be irregular as indicated by measuring blood levels of said PPAR agonist and/or said p38 inhibitor in the patient.
  • the pharmaceutical combination according to the invention is administered once daily.
  • the PPAR agonist can be administered from 0.1 - 100 mg per day and the P38 inhibitor can be administered from 1 - 300 mg per day.
  • the present invention provides a pharmaceutical combination as described herein, for use as a medicament.
  • the present invention provides a pharmaceutical combination as described herein, for use in a method for the prevention, delay of progression or treatment of cancer in a subject.
  • treatment includes: (1) delaying the appearance of clinical symptoms of the state, disorder or condition developing in an animal, particularly a mammal and especially a human, that may be afflicted with or predisposed to the state, disorder or condition but does not yet experience or display clinical or subclinical symptoms of the state, disorder or condition; (2) inhibiting the state, disorder or condition (e.g. arresting, reducing or delaying the development of the disease, or a relapse thereof in case of maintenance treatment, of at least one clinical or subclinical symptom thereof); and/or (3) relieving the condition (i.e. causing regression of the state, disorder or condition or at least one of its clinical or subclinical symptoms).
  • the benefit to a patient to be treated is either statistically significant or at least perceptible to the patient or to the physician. However, it will be appreciated that when a medicament is administered to a patient to treat a disease, the outcome may not always be effective treatment.
  • delay of progression means increasing the time to appearance of a symptom of a cancer or a mark associated with a cancer or slowing the increase in severity of a symptom of a cancer. Further, “delay of progression” as used herein includes reversing or inhibition of disease progression. “Inhibition" of disease progression or disease complication in a subject means preventing or reducing the disease progression and/or disease complication in the subject.
  • Preventive treatments comprise prophylactic treatments.
  • the pharmaceutical combination of the invention is administered to a subject suspected of having, or at risk for developing cancer.
  • the pharmaceutical combination is administered to a subject such as a patient already suffering from cancer, in an amount sufficient to cure or at least partially arrest the symptoms of the disease. Amounts effective for this use will depend on the severity and course of the disease, previous therapy, the subject's health status and response to the drugs, and the judgment of the treating physician.
  • the pharmaceutical combination of the invention may be administered chronically, which is, for an extended period of time, including throughout the duration of the subject's life in order to ameliorate or otherwise control or limit the symptoms of the subject's disease or condition.
  • the pharmaceutical combination may be administered continuously; alternatively, the dose of drugs being administered may be temporarily reduced or temporarily suspended for a certain length of time (i.e., a "drug holiday").
  • a maintenance dose of the pharmaceutical combination of the invention is administered if necessary. Subsequently, the dosage or the frequency of administration, or both, is optionally reduced, as a function of the symptoms, to a level at which the improved disease is retained.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of cancer in a subject, wherein the cancer is selected from the group consisting of lung cancer, ovarian cancer, prostate cancer, breast cancer, bladder cancer, liver cancer, cancer of the gastrointestinal (GI) tract, hematological cancer and kidney cancer.
  • the cancer is selected from the group consisting of lung cancer, ovarian cancer, prostate cancer, breast cancer, bladder cancer, liver cancer, cancer of the gastrointestinal (GI) tract, hematological cancer and kidney cancer.
  • GI gastrointestinal
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer, ovarian cancer or of cancer of the gastrointestinal (GI) tract in a subject.
  • GI gastrointestinal
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer, ovarian cancer or of cancer of the gastrointestinal (GI) tract in a subject, wherein said lung cancer is selected from non-small-cell lung carcinoma and small-cell lung carcinoma and is preferably non-small-cell lung carcinoma, wherein said ovarian cancer is preferably epithelial-derived ovarian cancer and wherein said cancer of the GI tract is selected from esophageal cancer, gastric cancer, intestinal cancer, colorectal cancer, and anal cancer, and is preferably colorectal cancer.
  • GI gastrointestinal
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer or of cancer of the gastrointestinal (GI) tract in a subject.
  • GI gastrointestinal
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer or of cancer of the gastrointestinal (GI) tract in a subject, wherein said lung cancer is selected from non-small-cell lung carcinoma and small-cell lung carcinoma and is preferably non-small-cell lung carcinoma and wherein said cancer of the GI tract is selected from esophageal cancer, gastric cancer, intestinal cancer, colorectal cancer, and anal cancer, and is preferably colorectal cancer.
  • GI gastrointestinal
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of breast cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of bladder cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of liver cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of cancer of the GI tract in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of hematological cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of kidney cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer in a subject, wherein said lung cancer is selected from non-small-cell lung carcinoma and small-cell lung carcinoma.
  • said lung cancer is non-small-cell lung carcinoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of ovarian cancer in a subject, wherein said ovarian cancer is preferably epithelial-derived ovarian cancer.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of prostate cancer in a subject, wherein said prostate cancer is preferably acinar adenocarcinoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of breast cancer in a subject, wherein said breast cancer is selected from ductal carcinoma in situ, invasive ductal carcinoma and invasive lobular carcinoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of bladder cancer in a subject, wherein said bladder cancer is selected from transitional cell carcinoma, squamous cell carcinoma, small cell carcinoma, adenocarcinoma and sarcoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of liver cancer in a subject, wherein said liver cancer is selected from hepatocellular carcinoma, hepatoblastoma and cholangiocarcinoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of cancer of the GI tract in a subject, wherein said cancer of the GI tract is selected from esophageal cancer, gastric cancer, intestinal cancer, colorectal cancer, and anal cancer.
  • said cancer of the GI tract is colorectal cancer.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of hematological cancer in a subject, wherein said hematological cancer is selected from acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), chronic lymphocytic leukemia (CLL), lymphoma, myelodysplastic syndrome (MDS) and multiple myeloma.
  • AML acute myeloid leukemia
  • ALL acute lymphoblastic leukemia
  • CML chronic myeloid leukemia
  • CLL chronic lymphocytic leukemia
  • MDS myelodysplastic syndrome
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of kidney cancer in a subject, wherein said kidney cancer is renal cell adenocarcinoma.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of lung cancer or ovarian cancer in a subject.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of cancer in a subject, wherein the cancer is selected from the group consisting of cancer of the GI tract, hematological cancer and kidney cancer.
  • a pharmaceutical combination according to the invention for use in a method for the prevention, delay of progression or treatment of metastatic cancer, preferably metastatic cancer selected from the group consisting of metastatic lung cancer, metastatic ovarian cancer, metastatic prostate cancer, metastatic breast cancer, metastatic bladder cancer, metastatic liver cancer, metastatic cancer of the gastrointestinal (GI) tract, and metastatic kidney cancer, more preferably metastatic cancer of the GI tract, metastatic ovarian cancer or metastatic lung cancer, even more preferably metastatic cancer of the GI tract or metastatic lung cancer, most preferably metastatic cancer of the GI tract selected from metastatic esophageal cancer, metastatic gastric cancer, metastatic intestinal cancer, metastatic colorectal cancer, and metastatic anal cancer, in particular metastatic colorectal cancer, or metastatic lung cancer selected from metastatic non-small-cell lung carcinoma and metastatic small-cell lung carcinoma, in particular metastatic non-small-cell lung carcinoma, in a subject.
  • metastatic cancer selected from the group consisting of metastatic lung cancer, metastatic ova
  • the present invention provides a pharmaceutical combination comprising:
  • PPAR agonists are as defined above.
  • said PPAR agonist is a PPAR gamma agonist, in particular pioglitazone or a pharmaceutically acceptable salt thereof.
  • the p38 kinase inhibitors are compunds of the formula I or II as defined; supra
  • pamapimod and/or R9111 in particular pamapimod and/or R9111, more particular pamapimod or a pharmaceutically acceptable salt thereof.
  • Lung cancers or ovarian cancers are as defined as above.
  • Preferred lung cancers are non-small-cell lung carcinoma or small-cell lung carcinoma and more preferably non-small-cell lung carcinoma and preferred ovarian cancer is epithelial-derived ovarian cancer.
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • the present invention provides a pharmaceutical combination comprising:
  • PPAR agonists are as defined above.
  • said PPAR agonist is a PPAR gamma agonist, in particular pioglitazone or a pharmaceutically acceptable salt thereof.
  • the p38 kinase inhibitors are compunds of the formula I or II as defined supra
  • pamapimod and/or R9111 in particular pamapimod and/or R9111, more particular pamapimod or a pharmaceutically acceptable salt thereof.
  • Lung cancers or cancers of the GI tract are as defined as above.
  • Preferred lung cancers are non-small-cell lung carcinoma or small-cell lung carcinoma, and more preferably non-small-cell lung carcinoma and preferred cancers of the GI tract are selected from esophageal cancer, gastric cancer, intestinal cancer, colorectal cancer, and anal cancer, and more preferably colorectal cancer.
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • a pharmaceutical combination comprising:
  • MS-Excel 2003 On the following day (day 22), treatment was initiated in all groups (see Table 1 for details).
  • Pioglitazone HCL (10 mg/kg) and pamapimod (100 mg/kg) were administered both alone (Groups 2 and 3, respectively) and in combination (Group 4) once daily p.o. on days 22-45.
  • Animals of Group 1 were treated with 10 ml/kg Vehicle Control (0.9% NaCl, 0.5% Methyl Cellulose, 0.4% polysorbate 80, 0.9% benzyl alcohol, pH 4.8) once daily p.o. for the same time period.
  • Table 1 Study design Group Compound Dose Route Scheme Number of animals 1 Vehicle Control 1) 10 ml/kg p.o. 1x daily on days 22-45 10 2 pioglitazone HCl 10 mg/kg p.o. 1x daily on days 22-45 10 3 pamapimod 100 mg/kg p.o. 1x daily on days 22-45 10 4 pioglitazone HCl + pamapimod 10 mg/kg + 100 mg/kg p.o. 1x daily on days 22-45 10 1) 0.9% NaCl, 0.5% Methyl Cellulose, 0.4% polysorbate 80, 0.9% benzyl alcohol, pH 4.8
  • Target cells tumor cells for implantation
  • A549 cells were grown in DMEM high Glutamax 1 with 10% FCS, 100 units penicillin/ml, and 100 ⁇ g of streptomycin/ml. A549 cells were cultured in a humidified atmosphere of 90% air and 10% carbon dioxide at 37°C. Media were routinely changed every 3 days.
  • tumor-bearing animals were block-randomized into 4 groups of 10 animals each according to the latest primary tumor measurements (block of four after ranking). For block randomization, a robust automated random number generation within individual blocks was used (MS-Excel 2003). On the following day (day 22), treatment was initiated in all groups (see Table 1 for details).
  • the study consisted of four experimental groups, each containing containing 10 female athymic nude mice after randomization. On day 0, 2x10 6 A549 tumor cells were subcutaneously implanted into all animals. After randomization, treatment was initiated on day 22. Pioglitazone HCL and pamapimod were both administered alone (Groups 2 and 3, respectively) as well as in combination (Group 4) and evaluated versus their corresponding Vehicle Control (Group 1). On day 46, the study was terminated, i.e. all animals were sacrificed and a necropsy was performed to assess tumor growth.
  • MS-Excel 2016 a robust automated random number generation within individual blocks was used (MS-Excel 2016). Thereby, detected luciferase signals served as randomization criteria.
  • day 3 treatment was initiated in all groups (see Table 1 for details). All treatments were performed at 10 ml/kg 1x daily p.o. on days 3-20.
  • Pioglitazone HCL 25 mg/kg and pamapimod (100 mg/kg) were administered both alone (Groups 2 and 3, respectively) and in combination (Group 4) once daily p.o.
  • Animals of Group 1 were treated with 10 ml/kg Vehicle Control (0.9% NaCl, 0.5% Methyl Cellulose, 0.4% polysorbate 80, 0.9% benzyl alcohol, pH 4.8) once daily p.o.
  • Table 2 Study design Group Compound Dose Route Scheme Number of animals 1 Vehicle Control 2) 10 ml/kg p.o. 1x daily on days 3-20 12 2 pioglitazone HCl 25 mg/kg p.o. 1x daily on days 3-20 12 3 pamapimod 100 mg/kg p.o. 1x daily on days 3-20 12 4 pioglitazone HCl + pamapimod 25 mg/kg + 100 mg/kg p.o. + p.o. both: 1x daily on days 3-20 12 1) All animals listed here share the common suffix /16; 2) 0.9% NaCl, 0.5% Methyl Cellulose, 0.4% polysorbate 80, 0.9% benzyl alcohol, pH 4.8
  • Target cells tumor cells for implantation
  • CT26wt tumor cells were previously transfected in order to generate the firefly luciferase expressing cell line CT26wt_LLN.
  • CT26wt_LLN cells were grown in RPMI-1640 Glutamax 1, supplemented with 10% FCS, 100 units penicillin/ml and 100 ⁇ g of streptomycin/ml. Cells were routinely split every 3 days.
  • animal weights were measured three times weekly (Monday, Wednesday and Friday; balance: Mettler Toledo PB602-L). Primary tumor growth was monitored once weekly on days 2, 9, 15 and 20 using in vivo bioluminescence imaging. On day 2, 48 animals were randomized into 4 groups of 12 animals each according to the current in vivo bioluminescence imaging results (block of four after ranking). For block randomization, a robust automated random number generation within individual blocks was used (MS-Excel 2016). Thereby, detected luciferase signals served as randomization criteria. On the following day (day 3), treatment was initiated in all groups (see Table 2 for details).

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EP3468604A1 (en) 2019-04-17
AU2017277478B2 (en) 2023-03-16
US11285155B2 (en) 2022-03-29
CY1124123T1 (el) 2022-05-27
CA3023392A1 (en) 2017-12-14
KR102437685B1 (ko) 2022-08-29
CA3023392C (en) 2024-02-06
CN109414506B (zh) 2022-06-03
CN109414506A (zh) 2019-03-01
IL263407B (en) 2021-09-30
DK3468604T3 (da) 2021-04-19
CO2018013020A2 (es) 2018-12-28
PE20190376A1 (es) 2019-03-08
PH12018550186A1 (en) 2019-03-18
WO2017211830A1 (en) 2017-12-14
HUE053648T2 (hu) 2021-07-28
US20190160072A1 (en) 2019-05-30
JP7349790B2 (ja) 2023-09-25
MX2018014938A (es) 2019-05-16
JP2022046526A (ja) 2022-03-23
MY195671A (en) 2023-02-03
PT3468604T (pt) 2021-04-06
AU2017277478A1 (en) 2018-11-22
PL3468604T3 (pl) 2021-07-12
ES2866883T3 (es) 2021-10-20
EA201892287A1 (ru) 2019-06-28
ZA201900052B (en) 2021-10-27
KR20190017756A (ko) 2019-02-20
CN115105601A (zh) 2022-09-27
BR112018075135A2 (pt) 2019-03-26
IL263407A (en) 2018-12-31
UA123914C2 (uk) 2021-06-23
SG11201809882XA (en) 2018-12-28
JP2019517562A (ja) 2019-06-24
US20220175786A1 (en) 2022-06-09
CL2018003509A1 (es) 2019-03-15

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